{{Rsnum
|rsid=121908580
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BCS1L
|position=218661135
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BCS1L,ZNF142
}}{{omim
|id=603647
|rsnum=121908580
|variant=0011
}}{{ClinVar
|rsid=121908580
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=219525858
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ZNF142:7701; BCS1L:617
|GENE_NAME=ZNF142; BCS1L
|GENE_ID=7701; 617
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.219525858A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603647.0011
|CLNSIG=5
|CLNCUI=C1852372
|CLNDBN=Mitochondrial complex III deficiency
|Disease=Mitochondrial complex III deficiency
|CLNACC=RCV000006549.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1852372:124000:254902
}}